Species | Disruptability | Reference | Submitter | |
---|---|---|---|---|
P. falciparum 3D7 |
Possible |
USF piggyBac screen (Insert. mut.) | USF PiggyBac Screen | |
P. falciparum 3D7 |
Possible |
31559936 "PfDPY19 gene disruption was not associated with a growth phenotype, not even under endoplasmic reticulum (ER)-stressing conditions that could impair protein folding. The data presented in this work strongly suggests that PfDPY19 is unlikely to play a critical role in the asexual blood stages of the parasite, at least under in vitro conditions. " |
Theo Sanderson, Francis Crick Institute | |
P. falciparum 3D7 |
Possible |
35906227 \'We further show that genetic disruption of DPY19 in P. falciparum is necessary and sufficient to prevent C-mannosylation in the parasite, impair egress following gametocyte activation and abrogate ookinete infection of the mosquito midgut. Complementation of DPY19 restored the transmission defect and re-instated C-mannosylation activity, definitively validating tryptophan C-mannosylation as essential for P. falciparum infection of the mosquito, which is critical for onward transmission of the parasite.\' |
Theo Sanderson, Francis Crick Institute | |
P. berghei ANKA |
Possible |
RMgm-5209 | Imported from RMgmDB |
Species | Stage | Phenotype | Reference | Submitter |
---|---|---|---|---|
P. falciparum 3D7 | Asexual |
No difference |
31559936 "PfDPY19 gene disruption was not associated with a growth phenotype, not even under endoplasmic reticulum (ER)-stressing conditions that could impair protein folding. The data presented in this work strongly suggests that PfDPY19 is unlikely to play a critical role in the asexual blood stages of the parasite, at least under in vitro conditions. " |
Theo Sanderson, Francis Crick Institute |
P. falciparum 3D7 | Oocyst |
Attenuated |
35906227 \'We further show that genetic disruption of DPY19 in P. falciparum is necessary and sufficient to prevent C-mannosylation in the parasite, impair egress following gametocyte activation and abrogate ookinete infection of the mosquito midgut. Complementation of DPY19 restored the transmission defect and re-instated C-mannosylation activity, definitively validating tryptophan C-mannosylation as essential for P. falciparum infection of the mosquito, which is critical for onward transmission of the parasite.\' |
Theo Sanderson, Francis Crick Institute |
P. berghei ANKA | Asexual |
No difference |
RMgm-5209 | Imported from RMgmDB |
P. berghei ANKA | Gametocyte |
No difference |
RMgm-5209 | Imported from RMgmDB |
P. berghei ANKA | Ookinete |
Difference from wild-type |
RMgm-5209
Normal, wild-type gametocyte and ookinete production. However, ookinetes showed strongly reduced motility and motion velocity. No oocysts are formed |
Imported from RMgmDB |
P. berghei ANKA | Oocyst |
Difference from wild-type |
RMgm-5209
No oocyst formation |
Imported from RMgmDB |
P. berghei ANKA | Sporozoite |
Difference from wild-type |
RMgm-5209
No oocyst and sporozoite formation |
Imported from RMgmDB |
PlasmoDB | PF3D7_0806200 |
GeneDB | PF3D7_0806200 |
Malaria Metabolic Pathways | Localisation images Pathways mapped to |
Previous ID(s) | MAL8P1.135 |
Orthologs | PBANKA_1224500 , PCHAS_1225100 , PKNH_0112700 , PVP01_0114300 , PVX_088240 , PY17X_1227700 |
Google Scholar | Search for all mentions of this gene |